Identity

Trade Name
Diazyme FDA UDI
Generic Name
Kappa/lambda light chain immunoglobulin IVD, control FDA UDI
Model / Reference
08896577190 FDA UDI

Identifiers

Primary DI / UDI-DI
00817089023024 FDA UDI
GMDN Term
Kappa/lambda light chain immunoglobulin IVD, control FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Kappa/lambda light chain immunoglobulin IVD, control

Diazyme by Diazyme Laboratories, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Kappa/lambda light chain immunoglobulin IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e08061a3-9f9b-474a-b533-40ce3c36c885 32 fields · synced Jun 9, 2026